Allele Registry

Canonical Allele Identifier: PA278331

Gene: BTD HGNC NCBI

ClinVar Allele:

36396

ClinVar RCV:

RCV000022007

RCV000985644

ClinVar Variation:

25082

HGVS (amino-acid)	Matching Registered Transcripts
NP_000051.1:p.Gly445Val	CA278330 NM_000060.4:c.1334G>T